Related gene-specific medical variations for Gene (Select 10942) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3219820	NM_006799.4(PRSS21):c.47C>G (p.Ala16Gly)	LOC130058270, PRSS21 (A16G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219022	NM_006799.4(PRSS21):c.7G>A (p.Ala3Thr)	LOC130058270, PRSS21 (A3T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance